FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ARKIT HBA1C

K Number: K030553 · Decision Sep 2, 2003
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
18
Review Days
193

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ARKIT HBA1C
K Number
K030553
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arkray, Inc.
Date Received
February 21, 2003
Decision Date
September 2, 2003
Product Code
LCP
Advisory Committee
Hematology
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LCP Assay, Glycosylated Hemoglobin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LCP), ordered by most recent decision date.

View all

Other Clearances by Arkray, Inc.

K Number Device Name
K232416 AUTION EYE AI-4510 Urine Particle Analysis System
K193514 AUTION MAX AX-4060 Urinalysis System
K221175 Multi-Lancet Device 2, ReliOn Premier Lancing Device
K200788 Assure Titanium Blood Glucose Monitoring System
K160062 AUTION ELEVEN Semi-Automated Urinalysis System
K121456 AUTION HYBRID AU-4050 FULLY AUTOMATED INTEGRATED URINE ANALYZER SYSTEM; URIFLET S 9HA URINE TEST STRIPS; AUTION CONTROL
K093098 AUTION MAX MODEL AX-4030 URINALYSIS SYSTEM
K053401 SPOTCHEM II CHEMISTRY BASIC 1 AND CHEMISTRY BASIC 2 TESTS
K051648 SPOTCHEM II INOGANIC PHOSPHORUS, CPK AND URIC ACID TESTS
K051432 SPOTCHEM II TOTAL BILIRUBIN, TOTAL PROTEIN AND ALBUMIN TESTS
Search all 18 clearances from Arkray, Inc. →